4pwy

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{{STRUCTURE_4pwy| PDB=4pwy | SCENE= }}
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==Crystal structure of a Calmodulin-lysine N-methyltransferase fragment==
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===Crystal structure of a Calmodulin-lysine N-methyltransferase fragment===
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<StructureSection load='4pwy' size='340' side='right' caption='[[4pwy]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
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== Structural highlights ==
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==Disease==
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<table><tr><td colspan='2'>[[4pwy]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4PWY OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4PWY FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=MLI:MALONATE+ION'>MLI</scene>, <scene name='pdbligand=SAH:S-ADENOSYL-L-HOMOCYSTEINE'>SAH</scene>, <scene name='pdbligand=UNX:UNKNOWN+ATOM+OR+ION'>UNX</scene></td></tr>
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<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">CAMKMT, C2orf34, CLNMT ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Calmodulin-lysine_N-methyltransferase Calmodulin-lysine N-methyltransferase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.1.1.60 2.1.1.60] </span></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4pwy FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4pwy OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4pwy RCSB], [http://www.ebi.ac.uk/pdbsum/4pwy PDBsum]</span></td></tr>
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</table>
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== Disease ==
[[http://www.uniprot.org/uniprot/CMKMT_HUMAN CMKMT_HUMAN]] Atypical hypotonia - cystinuria syndrome;2p21 microdeletion syndrome without cystinuria;2p21 microdeletion syndrome.
[[http://www.uniprot.org/uniprot/CMKMT_HUMAN CMKMT_HUMAN]] Atypical hypotonia - cystinuria syndrome;2p21 microdeletion syndrome without cystinuria;2p21 microdeletion syndrome.
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== Function ==
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==Function==
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[[http://www.uniprot.org/uniprot/CMKMT_HUMAN CMKMT_HUMAN]] Catalyzes the trimethylation of 'Lys-116' in calmodulin.<ref>PMID:20975703</ref>
[[http://www.uniprot.org/uniprot/CMKMT_HUMAN CMKMT_HUMAN]] Catalyzes the trimethylation of 'Lys-116' in calmodulin.<ref>PMID:20975703</ref>
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== References ==
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==About this Structure==
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<references/>
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[[4pwy]] is a 1 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4PWY OCA].
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__TOC__
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</StructureSection>
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==Reference==
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<references group="xtra"/><references/>
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[[Category: Calmodulin-lysine N-methyltransferase]]
[[Category: Calmodulin-lysine N-methyltransferase]]
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[[Category: Arrowsmith, C H.]]
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[[Category: Human]]
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[[Category: Bountra, C.]]
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[[Category: Arrowsmith, C H]]
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[[Category: Brown, P J.]]
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[[Category: Bountra, C]]
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[[Category: Edwards, A M.]]
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[[Category: Brown, P J]]
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[[Category: Hong, B S.]]
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[[Category: Edwards, A M]]
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[[Category: Li, Y.]]
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[[Category: Hong, B S]]
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[[Category: SGC, Structural Genomics Consortium.]]
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[[Category: Li, Y]]
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[[Category: Tempel, W.]]
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[[Category: Structural genomic]]
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[[Category: Walker, J R.]]
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[[Category: Tempel, W]]
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[[Category: Walker, J R]]
[[Category: Methyl transferase]]
[[Category: Methyl transferase]]
[[Category: Sgc]]
[[Category: Sgc]]
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[[Category: Structural genomic]]
 
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[[Category: Structural genomics consortium]]
 
[[Category: Transferase]]
[[Category: Transferase]]

Revision as of 08:43, 5 January 2015

Crystal structure of a Calmodulin-lysine N-methyltransferase fragment

4pwy, resolution 1.90Å

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